Literature DB >> 21327842

Sudden cardiac death in a patient with lamin A/C mutation in the absence of dilated cardiomyopathy or conduction disease.

Philipp Ehlermann, Stephanie Lehrke, Theano Papavassiliu, Benjamin Meder, Martin Borggrefe, Hugo A Katus, Rainer Schimpf.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2011        PMID： 21327842     DOI： 10.1007/s00392-011-0289-0

Source DB:  PubMed          Journal:  Clin Res Cardiol        ISSN： 1861-0684            Impact factor:   5.460


× No keyword cloud information.
  30 in total

1.  Laminopathy presenting as familial atrial fibrillation.

Authors:  Britt Maria Beckmann; Elke Holinski-Feder; Maggie C Walter; Nadine Haserück; Christopher Reithmann; Martin Hinterseer; Arthur A Wilde; Stefan Kääb
Journal:  Int J Cardiol       Date:  2010-05-15       Impact factor: 4.164

2.  Images in cardiovascular medicine. Cardiomyopathy in a Duchenne muscular dystrophy carrier and her diseased son: similar pattern revealed by cardiovascular MRI.

Authors:  Ali Yilmaz; Hans-Jürgen Gdynia; Albert C Ludolph; Karin Klingel; Reinhard Kandolf; Udo Sechtem
Journal:  Circulation       Date:  2010-03-16       Impact factor: 29.690

3.  The frequency of familial dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy.

Authors:  V V Michels; P P Moll; F A Miller; A J Tajik; J S Chu; D J Driscoll; J C Burnett; R J Rodeheffer; J H Chesebro; H D Tazelaar
Journal:  N Engl J Med       Date:  1992-01-09       Impact factor: 91.245

4.  Natural history of dilated cardiomyopathy due to lamin A/C gene mutations.

Authors:  Matthew R G Taylor; Pamela R Fain; Gianfranco Sinagra; Misi L Robinson; Alastair D Robertson; Elisa Carniel; Andrea Di Lenarda; Teresa J Bohlmeyer; Debra A Ferguson; Gary L Brodsky; Mark M Boucek; Jean Lascor; Andrew C Moss; Wai Lun P Li; Gary L Stetler; Francesco Muntoni; Michael R Bristow; Luisa Mestroni
Journal:  J Am Coll Cardiol       Date:  2003-03-05       Impact factor: 24.094

Review 5.  Clinical and genetic issues in familial dilated cardiomyopathy.

Authors:  Emily L Burkett; Ray E Hershberger
Journal:  J Am Coll Cardiol       Date:  2005-04-05       Impact factor: 24.094

6.  Frequency and phenotypes of familial dilated cardiomyopathy.

Authors:  E Grünig; J A Tasman; H Kücherer; W Franz; W Kübler; H A Katus
Journal:  J Am Coll Cardiol       Date:  1998-01       Impact factor: 24.094

7.  Long-term outcome and risk stratification in dilated cardiolaminopathies.

Authors:  Michele Pasotti; Catherine Klersy; Andrea Pilotto; Nicola Marziliano; Claudio Rapezzi; Alessandra Serio; Savina Mannarino; Fabiana Gambarin; Valentina Favalli; Maurizia Grasso; Manuela Agozzino; Carlo Campana; Antonello Gavazzi; Oreste Febo; Massimiliano Marini; Maurizio Landolina; Andrea Mortara; Giovanni Piccolo; Mario Viganò; Luigi Tavazzi; Eloisa Arbustini
Journal:  J Am Coll Cardiol       Date:  2008-10-07       Impact factor: 24.094

8.  Differentiation of heart failure related to dilated cardiomyopathy and coronary artery disease using gadolinium-enhanced cardiovascular magnetic resonance.

Authors:  J A McCrohon; J C C Moon; S K Prasad; W J McKenna; C H Lorenz; A J S Coats; D J Pennell
Journal:  Circulation       Date:  2003-06-23       Impact factor: 29.690

9.  Malignant mutation in the lamin A/C gene causing progressive conduction system disease and early sudden death in a family with mild form of limb-girdle muscular dystrophy.

Authors:  Loizos Antoniades; Christos Eftychiou; Theodoros Kyriakides; Kyproula Christodoulou; Demosthenes G Katritsis
Journal:  J Interv Card Electrophysiol       Date:  2007-06-29       Impact factor: 1.900

10.  Lamin A/C truncation in dilated cardiomyopathy with conduction disease.

Authors:  Heather M MacLeod; Mary R Culley; Jill M Huber; Elizabeth M McNally
Journal:  BMC Med Genet       Date:  2003-07-10       Impact factor: 2.103
View more
  7 in total

1.  The Brazilian Society of Cardiology and Brazilian Society of Exercise and Sports Medicine Updated Guidelines for Sports and Exercise Cardiology - 2019.

Authors:  Nabil Ghorayeb; Ricardo Stein; Daniel Jogaib Daher; Anderson Donelli da Silveira; Luiz Eduardo Fonteles Ritt; Daniel Fernando Pellegrino Dos Santos; Ana Paula Rennó Sierra; Artur Haddad Herdy; Claúdio Gil Soares de Araújo; Cléa Simone Sabino de Souza Colombo; Daniel Arkader Kopiler; Filipe Ferrari Ribeiro de Lacerda; José Kawazoe Lazzoli; Luciana Diniz Nagem Janot de Matos; Marcelo Bichels Leitão; Ricardo Contesini Francisco; Rodrigo Otávio Bougleux Alô; Sérgio Timerman; Tales de Carvalho; Thiago Ghorayeb Garcia
Journal:  Arq Bras Cardiol       Date:  2019-03       Impact factor: 2.000

Review 2.  Precision medicine approach to genetic cardiomyopathy.

Authors:  K Filonenko; H A Katus; B Meder
Journal:  Herz       Date:  2017-08       Impact factor: 1.443

3.  [Clinical and genetic aspects of hypertrophic and dilated cardiomyopathy].

Authors:  B Meder; H A Katus
Journal:  Internist (Berl)       Date:  2012-04       Impact factor: 0.743

Review 4.  Complex roads from genotype to phenotype in dilated cardiomyopathy: scientific update from the Working Group of Myocardial Function of the European Society of Cardiology.

Authors:  Antoine Bondue; Eloisa Arbustini; Anna Bianco; Michele Ciccarelli; Dana Dawson; Matteo De Rosa; Nazha Hamdani; Denise Hilfiker-Kleiner; Benjamin Meder; Adelino F Leite-Moreira; Thomas Thum; Carlo G Tocchetti; Gilda Varricchi; Jolanda Van der Velden; Roddy Walsh; Stephane Heymans
Journal:  Cardiovasc Res       Date:  2018-08-01       Impact factor: 10.787

5.  Sudden cardiac death in the young: how can disease recognition and prevention in family members be improved?

Authors:  Rainer Schimpf; Katrin Yen; Martin Borggrefe
Journal:  Herzschrittmacherther Elektrophysiol       Date:  2012-09

6.  [Dilated cardiomyopathy].

Authors:  Philipp Ehlermann; Hugo A Katus
Journal:  Herzschrittmacherther Elektrophysiol       Date:  2012-09-26

7.  What Should the Cardiologist know about Lamin Disease?

Authors:  Philippe Charron; Eloisa Arbustini; Gisèle Bonne
Journal:  Arrhythm Electrophysiol Rev       Date:  2012-09
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.